نتایج جستجو برای: ert

تعداد نتایج: 1495  

2016
Marialuisa Alliegro Rita Ferla Edoardo Nusco Chiara De Leonibus Carmine Settembre Alberto Auricchio

Enzyme replacement therapy (ERT) is the standard of care for several lysosomal storage diseases (LSDs). ERT, however, requires multiple and costly administrations and has limited efficacy. We recently showed that a single high dose administration of adeno-associated viral vector serotype 8 (AAV2/8) is at least as effective as weekly ERT in a mouse model of mucopolysaccharidosis type VI (MPS VI)...

2014
Alícia Dorneles Dornelles Louise Lapagesse de Camargo Pinto Ana Carolina de Paula Carlos Eduardo Steiner Charles Marques Lourenço Chong Ae Kim Dafne Dain Gandelman Horovitz Erlane Marques Ribeiro Eugênia Ribeiro Valadares Isabela Goulart Isabel C. Neves de Souza João Ivanildo da Costa Neri Luiz Carlos Santana-da-Silva Luiz Roberto Silva Márcia Ribeiro Ruy Pires de Oliveira Sobrinho Roberto Giugliani Ida Vanessa Doederlein Schwartz

Mucopolysaccharidosis type I (MPS I) is a rare lysosomal disorder caused by deficiency of alpha-L-iduronidase. Few clinical trials have assessed the effect of enzyme replacement therapy (ERT) for this condition. We conducted an exploratory, open-label, non-randomized, multicenter cohort study of patients with MPS I. Data were collected from questionnaires completed by attending physicians at th...

2010
Yu-Feng Ren Yuan-Hong Gao Xin-Ping Cao Wei-Jun Ye Bin S Teh

BACKGROUND To compare the results of external beam radiotherapy in combination with 3D- computed tomography (CT)-implanted interstitial high dose rate brachytherapy (ERT/3D-HDR-BT) versus conventional external beam radiotherapy (ERT) for the treatment of stage T2b nasopharyngeal carcinoma (NPC). METHODS Forty NPC patients diagnosed with stage T2b NPC were treated with ERT/3D-HDR-BT under loca...

2010
Jérôme Stirnemann Nadia Belmatoug Corine Vincent Olivier Fain Bruno Fantin France Mentré

INTRODUCTION Known biomarkers of Gaucher-disease activity are platelets, chitotriosidase, angiotensin-converting enzyme (ACE), tartrate-resistant acid phosphatase (TRAP) and ferritin. The aim of this study was to retrospectively evaluate the frequency of bone events (BE) and biomarker changes during two periods: diagnosis to first enzyme-replacement therapy (ERT) and the latter to the closing d...

2015
Marieke Biegstraaten Reynir Arngrímsson Frederic Barbey Lut Boks Franco Cecchi Patrick B Deegan Ulla Feldt-Rasmussen Tarekegn Geberhiwot Dominique P Germain Chris Hendriksz Derralynn A Hughes Ilkka Kantola Nesrin Karabul Christine Lavery Gabor E Linthorst Atul Mehta Erica van de Mheen João P Oliveira Rossella Parini Uma Ramaswami Michael Rudnicki Andreas Serra Claudia Sommer Gere Sunder-Plassmann Einar Svarstad Annelies Sweeb Wim Terryn Anna Tylki-Szymanska Camilla Tøndel Bojan Vujkovac Frank Weidemann Frits A Wijburg Peter Woolfson Carla EM Hollak

INTRODUCTION Fabry disease (FD) is a lysosomal storage disorder resulting in progressive nervous system, kidney and heart disease. Enzyme replacement therapy (ERT) may halt or attenuate disease progression. Since administration is burdensome and expensive, appropriate use is mandatory. We aimed to define European consensus recommendations for the initiation and cessation of ERT in patients with...

Journal: :Journal of neuromuscular diseases 2015
Rosângela M Silva Carmen S C Mendes Carolina C Aranda Marco A Curiati Maret H Rand Sandra O Kyosen Edna T Sakata Sueli Canossa Beatriz J Frangipani Ana M Martins

Pompe disease is a progressive multisystem disease caused by a lysosomal acid α-glycosidase enzyme (GAA) defi ciency, resulting in lysosomal accumulation of glycogen. The late-onset form is characterized by progressive skeletal and respiratory muscle dysfunction leading to functional disability and impairment of quality of life. Enzyme replacement therapy (ERT) and treatments, such as protein-e...

2017
Rita Ortolano Federico Baronio Riccardo Masetti Arcangelo Prete Alessandra Cassio Andrea Pession

We readwith interest the article by TakashiM et al. that recently appeared inMGMReport. Becausemany open issues remain about the outcome of infantile Pompe disease (IPD), we describe here our experience with two IPD siblings born to related parents and treated with enzyme replacement therapy (ERT) in the symptomatic and the pre-symptomatic state. In the symptomatic child with severe respiratory...

Journal: :Mayo Clinic proceedings 2012
Toby N Weingarten Sam J Venus Francis X Whalen Brittany J Lyne Holly A Tempel Sarah A Wilczewski Bradly J Narr David P Martin Darrell R Schroeder Juraj Sprung

OBJECTIVE To study characteristics and outcomes associated with emergency response team (ERT) activation in postsurgical patients discharged to regular wards after anesthesia. PATIENTS AND METHODS We identified all ERT activations that occurred within 48 hours after surgery from June 1, 2008, through December 31, 2009, in patients discharged from the postanesthesia care unit to regular wards....

اسحاقی, محبوبه , باستانی, سوسن , ساعی, علی , محمدفام, ایرج , گلمحمدی, رستم ,

Introduction: Emergency situations are of the major challenges in industries. Understading the status of inter-team interaction is effective in improvement of emergency response team (ERT). The purpose of this study was to investigate the interaction space of ERP in a refinery, using the social network analysis (SNA). .Methods and Materials: In the present case study, the density indicator was ...

2013
Divair Doneda Cristina B Netto Cileide C Moulin Ida Vanessa D Schwartz

BACKGROUND Gaucher disease (GD) type I is the most common type of GD. Its main clinical manifestations are hepatosplenomegaly as well as bone and hematological abnormalities. The objective of the present study was to perform a literature review on the growth and metabolism of GD type I patients. METHODS We searched Pubmed and Scielo.br databases with predetermined study limits: case series (n...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید